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Human Disease

3MC syndrome 1

Term ID
DOID:0060575
Synonyms
Definition
A 3MC syndrome that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the mannan binding lectin serine peptidase 1 gene (MASP1) on chromosome 3q27. (2)
References
Ontology
Human Disease   ( DOID:0060575 )
Relationships
is a type of
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Genes Involved
Zebrafish Models